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Thalassaemia trait with gaucher disease: A diagnostic dilemma
Jyoti Ramnath Kini
,
Saraswathy Sreeram
*
,
Anupama Hegde
,
Sowmini Kamath
, Radha Ramachandra Pai
*
Corresponding author for this work
Department of Pathology, Kasturba Medical College, Mangalore
Department of Biochemistry, Kasturba Medical College, Mangalore
Department of Paediatrics, Kasturba Medical College, Manipal
Research output
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Contribution to journal
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Article
›
peer-review
2
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Citations (Scopus)
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Medicine and Dentistry
Diagnosis
100%
Thalassemia
100%
Gaucher's Disease
100%
Glucosylceramidase
42%
Splenomegaly
28%
High-Performance Liquid Chromatography
14%
Thrombocytopenia
14%
Clinical Examination
14%
Weakness
14%
Hepatomegaly
14%
Splenectomy
14%
Anemia
14%
Hemolytic
14%
Failure to Thrive
14%
Sphingolipidoses
14%
Hepatosplenomegaly
14%
Mycobacterial Infection
14%
Pallor
14%
Myeloma
14%
Liver Biopsy
14%
Hemoglobinopathy
14%
Hemoglobin Variant
14%
Gaucher Disease Type 1
14%
Leukemia
14%
Autosomal Recessive Disorder
14%
Pharmacology, Toxicology and Pharmaceutical Science
Thalassemia
100%
Gaucher's Disease
100%
Glucosylceramidase
42%
Splenomegaly
28%
High Performance Liquid Chromatography
14%
Leukemia
14%
Infection
14%
Weakness
14%
Myeloma
14%
Hepatosplenomegaly
14%
Pallor
14%
Autosomal Recessive Disorder
14%
Failure to Thrive
14%
Phospholipidosis
14%
Gaucher Disease Type 1
14%
Anemia
14%
Thrombocytopenia
14%
Hemoglobin Variant
14%
Hepatomegaly
14%
Hemoglobinopathy
14%
INIS
diseases
100%
thalassemia
100%
patients
25%
liver
25%
bone marrow
25%
children
12%
management
12%
blood
12%
hemoglobin
12%
failures
12%
spleen
12%
storage
12%
lipids
12%
accumulation
12%
high-performance liquid chromatography
12%
anemias
12%
leukemia
12%
biopsy
12%
splenectomy
12%
splenomegaly
12%